chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134773926547739266AG8GENICheterozygous50458290
134773940047739401AC10GENIChomozygous49751928
134773962347739624TC12GENIChomozygous49751929
134773965547739656TC14GENICpossibly homozygous49751930
134774008847740089CT5GENICheterozygous49751931
134774031347740314GA19GENICpossibly homozygous49751932
134774035847740359AG12GENIChomozygous49751933
134774037447740375AG8GENIChomozygous49751934
134774037647740377GA8GENICheterozygous49751935
134774052647740527TC11GENIChomozygous49751936
134774052947740530AC9GENIChomozygous49751937
134774078747740788AG14GENICheterozygous49751938
134774100347741004CT16GENICpossibly homozygous49751940
134774103147741032TC17GENIChomozygous49751941
134774122747741228GA7GENIChomozygous49751942
134774150347741504CA19GENICpossibly homozygous49751943
134774173447741735GT12GENIChomozygous49751944
134774190247741903GA10GENICpossibly homozygous49751945
134774233347742355GTGTGTGTGTATGTGTGTGTGT----------------------7GENICpossibly homozygous49751946
134774286247742863TC9GENICpossibly homozygous49751950
134774287247742873GA5GENIChomozygous49751951
134774288347742884AG5GENIChomozygous49751952
134774295147742952GA14GENIChomozygous49751953
134774306747743068C-10GENIChomozygous49751954
134774326947743270GT7GENIChomozygous49751955
134774334847743349AG6GENIChomozygous49751956
134774335547743356AC7GENIChomozygous49751957